A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527522



Internal ID15454815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:84252173..84272997hg38UCSC Ensembl
Innerchr10:86011929..86032753hg19UCSC Ensembl
Innerchr10:86001909..86022733hg18UCSC Ensembl
Innerchr10:86001909..86022733hg17UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3820825
hg1920825
hg1820825
hg1720825
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703976
Samples
Known GenesRGR
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527522
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer